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Volumn 71, Issue 10, 2005, Pages 923-927

Cytotoxic and genotoxic butanolides and lignans from Aiouea trinervis

Author keywords

( ) Epilitsenolides C1 and C 2; Aiouea trinervis; Comet assay; Cytotoxic activity; Genotoxic activity; Lauraccae

Indexed keywords

AIOUEA TRINERVIS EXTRACT; BUTYROLACTONE; EPILITSENOLIDE C1; EPILITSENOLIDE C2; ISOOBTUSILACTONE A; LIGNAN DERIVATIVE; METHYLPIPERITOL; OBTUSILACTONE A; PLANT EXTRACT; POLYPRENOL 12; SESAMIN; UNCLASSIFIED DRUG;

EID: 27844504765     PISSN: 00320943     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2005-871251     Document Type: Article
Times cited : (28)

References (19)
  • 1
    • 0019849144 scopus 로고
    • The total synthesis of lauraceae lactones: Obtusilactones, litsenolides, and mahubanolides
    • Rollinson SW, Amos RA, Katzenellenbogen JA. The total synthesis of Lauraceae lactones: obtusilactones, litsenolides, and mahubanolides. J Am Chem Soc 1981; 103: 4114-25
    • (1981) J Am Chem Soc , vol.103 , pp. 4114-4125
    • Rollinson, S.W.1    Amos, R.A.2    Katzenellenbogen, J.A.3
  • 2
    • 0033874903 scopus 로고    scopus 로고
    • Efficient total synthesis of (-)-epilitsenolide C2 and (-)-isodihydromahubanolide B via a modified tungsten-mediated cycloalkenylation reaction
    • Chen M, Lo C, Liu R. Efficient total synthesis of (-)-epilitsenolide C2 and (-)-isodihydromahubanolide B via a modified tungsten-mediated cycloalkenylation reaction. Synlett 2000: 1205-7
    • (2000) Synlett , pp. 1205-1207
    • Chen, M.1    Lo, C.2    Liu, R.3
  • 3
    • 0036179825 scopus 로고    scopus 로고
    • Cytotoxic butanolides and secobutanolides from the stem wood of formosan lindera communis
    • Tsai I, Hung C, Duh C, Chen I. Cytotoxic butanolides and secobutanolides from the stem wood of Formosan Lindera communis. Planta Med 2002; 68: 142-5
    • (2002) Planta Med , vol.68 , pp. 142-145
    • Tsai, I.1    Hung, C.2    Duh, C.3    Chen, I.4
  • 4
    • 0026518266 scopus 로고
    • Biologically active γ-lactones and methylketoalkenes from lindera benzoin
    • Anderson JE, Ma W, Smith DL, Chang C, McLaughlin JL. Biologically active γ-lactones and methylketoalkenes from Lindera benzoin. J Nat Prod 1992; 55: 71-83
    • (1992) J Nat Prod , vol.55 , pp. 71-83
    • Anderson, J.E.1    Ma, W.2    Smith, D.L.3    Chang, C.4    McLaughlin, J.L.5
  • 6
    • 45949123799 scopus 로고
    • A cytotoxic tetralone derivative from parasistolochia flos-avis
    • Sun N, Chang C, Cassady JM. A cytotoxic tetralone derivative from Parasistolochia flos-avis. Phytochemistry 1987; 26: 3051-3
    • (1987) Phytochemistry , vol.26 , pp. 3051-3053
    • Sun, N.1    Chang, C.2    Cassady, J.M.3
  • 7
    • 84986749675 scopus 로고
    • 13C NMR spectroscopy of lignan and neolignan derivatives
    • 13C NMR spectroscopy of lignan and neolignan derivatives. Magn Reson Chem 1985; 23: 389-418
    • (1985) Magn Reson Chem , vol.23 , pp. 389-418
    • Agrawal, P.K.1    Thakur, R.S.2
  • 10
    • 0021061819 scopus 로고
    • Rapid colorimetric assay for cellular growth and survival: Application to proliferation and cytotoxicity assays
    • Mosmann T. Rapid colorimetric assay for cellular growth and survival: application to proliferation and cytotoxicity assays. J Immunol Methods 1983; 65: 55-63
    • (1983) J Immunol Methods , vol.65 , pp. 55-63
    • Mosmann, T.1
  • 11
    • 0023919963 scopus 로고
    • A simple technique for quantification of low levels of DNA damage in individual cells
    • Singh NP, McCoy MT, Tice RR, Schneider El. A simple technique for quantification of low levels of DNA damage in individual cells. Exp Cell Res 1988; 175: 184-91
    • (1988) Exp Cell Res , vol.175 , pp. 184-191
    • Singh, N.P.1    McCoy, M.T.2    Tice, R.R.3    Schneider, E.4
  • 14
    • 0035742504 scopus 로고    scopus 로고
    • Synthesis of oxygen heterocycles via alkynyltungsten compounds
    • Liu R. Synthesis of oxygen heterocycles via alkynyltungsten compounds. Pure Appl Chem 2001; 73: 265-9
    • (2001) Pure Appl Chem , vol.73 , pp. 265-269
    • Liu, R.1
  • 15
    • 0001732706 scopus 로고
    • Components of the Lauraceae family - I. New lactonic compounds from litsea japonica
    • Takeda K, Sakurawi K, Ishii H. Components of the Lauraceae family - I. New lactonic compounds from Litsea japonica. Tetrahedron 1972; 28: 3757-66
    • (1972) Tetrahedron , vol.28 , pp. 3757-3766
    • Takeda, K.1    Sakurawi, K.2    Ishii, H.3
  • 17
    • 0010027864 scopus 로고
    • Three new obtusilactones from lindera obtusiloba blume
    • Niwa M, Iguchi M, Yamamura S. Three new obtusilactones from Lindera obtusiloba Blume. Chem Lett 1975: 655-8
    • (1975) Chem Lett , pp. 655-658
    • Niwa, M.1    Iguchi, M.2    Yamamura, S.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.